Hoving, Jan W. http://orcid.org/0000-0003-3310-3973
Kappelhof, Manon http://orcid.org/0000-0001-5250-8955
Schembri, Mark http://orcid.org/0000-0002-3611-2771
Emmer, Bart J. http://orcid.org/0000-0001-8462-4037
Berkhemer, Olvert A. http://orcid.org/0000-0002-2212-6128
Groot, Adrien E. D. http://orcid.org/0000-0002-6079-8603
Dippel, Diederik W. J. http://orcid.org/0000-0002-9234-3515
van Zwam, Wim H. http://orcid.org/0000-0003-1631-7056
Coutinho, Jonathan M. http://orcid.org/0000-0002-8284-982X
Marquering, Henk A. http://orcid.org/0000-0002-1414-6313
Majoie, Charles B. L. M. http://orcid.org/0000-0002-7600-9568
van den Berg, René http://orcid.org/0000-0002-8791-8791
,
Funding for this research was provided by:
Amsterdam UMC
Article History
Received: 15 May 2020
Accepted: 6 September 2020
First Online: 7 October 2020
Compliance with ethical standards
:
: BJE reports grants from Stryker Neurovascular and personal fees from Dekra and from Novartis outside the submitted work. CBLMM reports grants from TWIN during the conduct of the study and grants from CVON/Dutch Heart Foundation and from Stryker outside the submitted work (paid to institution). WHvZ reports personal fees from Cerenovus and from Stryker outside the submitted work. RvdB reports a consultancy agreement with Codman Depuy outside the submitted work. DWJD reports grants from the Dutch Heart Foundation, AngioCare, Medtronic/Covidien/EV3, MEDAC/LAMEPRO, Penumbra, Top Medical/Concentric, and Stryker during conduct of the study; consultation fees from Stryker, Bracco Imaging, and Servier, received by the Erasmus University Medical Centre, outside the submitted work. All other authors did not receive support from any organization for the submitted work, had no financial relationships with any organizations that might have an interest in the submitted work in the previous three years, and had no other relationships or activities that could appear to have influenced the submitted work.
: The MR CLEAN Registry was evaluated by the central medical ethics committee of the Erasmus Medical Centre Rotterdam, the Netherlands, which granted permission to carry out the study as a Registry.
: For this type of study, formal consent is not required. For included patients from the MR CLEAN trial, informed consent was obtained.
: No identifying data was included in the current study.
: The data to reproduce or replicate the findings of this study cannot be made available since no patient approval was collected for sharing coded data. Summary data, syntaxes, and output files of summary statistics are available upon reasonable request.
: Syntaxes and output files of summary statistics are available upon reasonable request.